Identification of a mutation in the promoter region of the dystrophin gene in a patient with atypical Becker muscular dystrophy
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Figure 7 from Spectrum of mutations in Duchenne Muscular Dystrophy (DMD) and clinical phenotype correlation in Sri Lankan population. | Semantic Scholar
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PDF) Association between the SMN2 gene copy number and clinical characteristics of patients with spinal muscular atrophy with homozygous deletion of exon 7 of the SMN1 gene
Diagnosis and New Treatment Avenues in Spinal Muscular Atrophy
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Breathing in Duchenne muscular dystrophy: translation to therapy - Mhandire - 2022 - The Journal of Physiology - Wiley Online Library
Figure 5 from Spectrum of mutations in Duchenne Muscular Dystrophy (DMD) and clinical phenotype correlation in Sri Lankan population. | Semantic Scholar
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Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy. - Abstract - Europe PMC
